{"title":"Metalloligand-anion frameworks: Tunable polarized luminescence and crystal-to-crystal transformation","authors":"","doi":"10.1016/j.matt.2024.06.012","DOIUrl":null,"url":null,"abstract":"<div><div><span><span>Noncovalent organic frameworks (NCOFs) are porous materials constructed by diverse intermolecular interactions. It is challenging to obtain polymorphic NCOFs with adjustable pores and high-performance </span>polarized luminescence<span>. Here, two polymorphic organometallic NCOFs, </span></span><strong>1</strong>-<em>α</em> and <strong>1</strong>-<em>β</em><span>, are presented from an iridium complex </span><strong>1</strong><span><span> based on the intralayer F···H hydrogen bonding and interlayer cation-anion </span>electrostatic interactions<span>. These metalloligand-anion frameworks display linearly polarized blue phosphorescence with a polarization degree of up to 0.91 and optical waveguide properties. The </span></span><strong>1</strong>-<em>α</em><span> microcrystals<span> doped with a ruthenium acceptor manifest a reversible response to Et</span></span><sub>2</sub>O vapor, showing modulated energy transfer and polarized luminescence. The <strong>1</strong>-<em>α</em> and <strong>1</strong>-<em>β</em><span> microcrystals are transformed into another polymorphic </span><strong>1</strong>-<em>γ</em> crystal by incorporating chiral (<em>R</em>/<em>S</em><span>)-carvone guests, affording tunable circularly polarized luminescence with a dissymmetry factor of around 0.1. This work provides a unique concept to obtain polymorphic NCOFs, demonstrating prominent potential in multifunctional optical and chiroptical applications.</span></div></div>","PeriodicalId":388,"journal":{"name":"Matter","volume":"7 10","pages":"Pages 3537-3553"},"PeriodicalIF":17.3000,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Matter","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S259023852400331X","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Noncovalent organic frameworks (NCOFs) are porous materials constructed by diverse intermolecular interactions. It is challenging to obtain polymorphic NCOFs with adjustable pores and high-performance polarized luminescence. Here, two polymorphic organometallic NCOFs, 1-α and 1-β, are presented from an iridium complex 1 based on the intralayer F···H hydrogen bonding and interlayer cation-anion electrostatic interactions. These metalloligand-anion frameworks display linearly polarized blue phosphorescence with a polarization degree of up to 0.91 and optical waveguide properties. The 1-α microcrystals doped with a ruthenium acceptor manifest a reversible response to Et2O vapor, showing modulated energy transfer and polarized luminescence. The 1-α and 1-β microcrystals are transformed into another polymorphic 1-γ crystal by incorporating chiral (R/S)-carvone guests, affording tunable circularly polarized luminescence with a dissymmetry factor of around 0.1. This work provides a unique concept to obtain polymorphic NCOFs, demonstrating prominent potential in multifunctional optical and chiroptical applications.
期刊介绍:
Matter, a monthly journal affiliated with Cell, spans the broad field of materials science from nano to macro levels,covering fundamentals to applications. Embracing groundbreaking technologies,it includes full-length research articles,reviews, perspectives,previews, opinions, personnel stories, and general editorial content.
Matter aims to be the primary resource for researchers in academia and industry, inspiring the next generation of materials scientists.